Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction

Renal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enro...

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Main Authors: Hee-Sung Ahn, Jong Ho Kim, Hwangkyo Jeong, Jiyoung Yu, Jeonghun Yeom, Sang Heon Song, Sang Soo Kim, In Joo Kim, Kyunggon Kim
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/12/4236
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spelling doaj-41b1dc6bec31436bbc0386c67b1611992020-11-25T03:38:25ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-06-01214236423610.3390/ijms21124236Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal DysfunctionHee-Sung Ahn0Jong Ho Kim1Hwangkyo Jeong2Jiyoung Yu3Jeonghun Yeom4Sang Heon Song5Sang Soo Kim6In Joo Kim7Kyunggon Kim8Asan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Biomedical Sciences, University of Ulsan College of Medicine, Seoul 05505, KoreaAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaConvergence Medicine Research Center, Asan Institute for Life Sciences, Seoul 05505, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaDepartment of Internal Medicine, Pusan National University Hospital, Pusan 49241, KoreaAsan Institute for Life Sciences, Asan Medical Center, Seoul 05505, KoreaRenal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enrolled in the retrospective diabetic kidney disease (DKD) study, including 35 with good and 19 with poor prognosis. After removal of albumin and immunoglobulin, the remaining proteins were reduced, alkylated, digested, and analyzed qualitatively and quantitatively with a nano LC-MS platform. Each protein was identified, and its concentration normalized to that of creatinine. A prognostic model of DKD was formulated based on the adjusted quantities of each protein in the two groups. Of 1296 proteins identified in the 54 urine samples, 66 were differentially abundant in the two groups (area under the curve (AUC): <i>p</i>-value < 0.05), but none showed significantly better performance than albumin. To improve the predictive power by multivariate analysis, five proteins (ACP2, CTSA, GM2A, MUC1, and SPARCL1) were selected as significant by an AUC-based random forest method. The application of two classifiers—support vector machine and random forest—showed that the multivariate model performed better than univariate analysis of mucin-1 (AUC: 0.935 vs. 0.791) and albumin (AUC: 1.0 vs. 0.722). The urinary proteome can reflect kidney function directly and can predict the prognosis of patients with chronic kidney dysfunction. Classification based on five urinary proteins may better predict the prognosis of DKD patients than urinary albumin concentration or eGFR.https://www.mdpi.com/1422-0067/21/12/4236urinediabetic kidney diseasekidney functionproteomicsmass spectrometrystatistical clinical model
collection DOAJ
language English
format Article
sources DOAJ
author Hee-Sung Ahn
Jong Ho Kim
Hwangkyo Jeong
Jiyoung Yu
Jeonghun Yeom
Sang Heon Song
Sang Soo Kim
In Joo Kim
Kyunggon Kim
spellingShingle Hee-Sung Ahn
Jong Ho Kim
Hwangkyo Jeong
Jiyoung Yu
Jeonghun Yeom
Sang Heon Song
Sang Soo Kim
In Joo Kim
Kyunggon Kim
Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
International Journal of Molecular Sciences
urine
diabetic kidney disease
kidney function
proteomics
mass spectrometry
statistical clinical model
author_facet Hee-Sung Ahn
Jong Ho Kim
Hwangkyo Jeong
Jiyoung Yu
Jeonghun Yeom
Sang Heon Song
Sang Soo Kim
In Joo Kim
Kyunggon Kim
author_sort Hee-Sung Ahn
title Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
title_short Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
title_full Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
title_fullStr Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
title_full_unstemmed Differential Urinary Proteome Analysis for Predicting Prognosis in Type 2 Diabetes Patients with and without Renal Dysfunction
title_sort differential urinary proteome analysis for predicting prognosis in type 2 diabetes patients with and without renal dysfunction
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-06-01
description Renal dysfunction, a major complication of type 2 diabetes, can be predicted from estimated glomerular filtration rate (eGFR) and protein markers such as albumin concentration. Urinary protein biomarkers may be used to monitor or predict patient status. Urine samples were selected from patients enrolled in the retrospective diabetic kidney disease (DKD) study, including 35 with good and 19 with poor prognosis. After removal of albumin and immunoglobulin, the remaining proteins were reduced, alkylated, digested, and analyzed qualitatively and quantitatively with a nano LC-MS platform. Each protein was identified, and its concentration normalized to that of creatinine. A prognostic model of DKD was formulated based on the adjusted quantities of each protein in the two groups. Of 1296 proteins identified in the 54 urine samples, 66 were differentially abundant in the two groups (area under the curve (AUC): <i>p</i>-value < 0.05), but none showed significantly better performance than albumin. To improve the predictive power by multivariate analysis, five proteins (ACP2, CTSA, GM2A, MUC1, and SPARCL1) were selected as significant by an AUC-based random forest method. The application of two classifiers—support vector machine and random forest—showed that the multivariate model performed better than univariate analysis of mucin-1 (AUC: 0.935 vs. 0.791) and albumin (AUC: 1.0 vs. 0.722). The urinary proteome can reflect kidney function directly and can predict the prognosis of patients with chronic kidney dysfunction. Classification based on five urinary proteins may better predict the prognosis of DKD patients than urinary albumin concentration or eGFR.
topic urine
diabetic kidney disease
kidney function
proteomics
mass spectrometry
statistical clinical model
url https://www.mdpi.com/1422-0067/21/12/4236
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